RAI1: Difference between revisions
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'''RAI1''' is a [[transcription factor]] associated with [[ |
'''RAI1''' is a [[transcription factor]] associated with [[Smith–Magenis syndrome]]. It is known as ''retinoic acid induced 1''. |
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==External links== |
==External links== |
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* [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms GeneReviews/NIH/NCBI/UW entry on Smith-Magenis Syndrome] |
* [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms GeneReviews/NIH/NCBI/UW entry on Smith-Magenis Syndrome] |
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* {{ |
* {{MeSH name|RAI1+protein,+human}} |
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Revision as of 16:57, 22 January 2020
| retinoic acid induced 1 | |||||||
|---|---|---|---|---|---|---|---|
| Identifiers | |||||||
| Symbol | RAI1 | ||||||
| NCBI gene | 10743 | ||||||
| HGNC | 9834 | ||||||
| OMIM | 607642 | ||||||
| RefSeq | NM_030665 | ||||||
| UniProt | Q7Z5J4 | ||||||
| Other data | |||||||
| Locus | Chr. 17 p11.2 | ||||||
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RAI1 is a transcription factor associated with Smith–Magenis syndrome. It is known as retinoic acid induced 1.
External links
- GeneReviews/NIH/NCBI/UW entry on Smith-Magenis Syndrome
- RAI1+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
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